Variant report

Variant	rs73037321
Chromosome Location	chr19:38765956-38765957
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:38763683..38766666-chr19:38812361..38813866,2	K562	blood:
2	chr19:38765937..38769216-chr19:38788492..38791727,3	MCF-7	breast:
3	chr19:38765291..38770264-chr19:38793708..38796948,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000167644	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs3885340	1.00[EUR][1000 genomes]
rs61734615	1.00[EUR][1000 genomes]
rs73037333	0.97[EUR][1000 genomes]
rs73037343	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73037346	1.00[EUR][1000 genomes]
rs73041292	1.00[EUR][1000 genomes]
rs73043012	0.87[EUR][1000 genomes]
rs73043013	0.87[EUR][1000 genomes]
rs73043014	0.87[EUR][1000 genomes]
rs73043015	0.87[EUR][1000 genomes]
rs73043019	0.87[EUR][1000 genomes]
rs73043021	0.87[EUR][1000 genomes]
rs73043022	0.87[EUR][1000 genomes]
rs73043027	0.87[EUR][1000 genomes]
rs73043028	0.87[EUR][1000 genomes]
rs73043029	0.84[EUR][1000 genomes]
rs73043030	0.84[EUR][1000 genomes]
rs73043033	0.84[EUR][1000 genomes]
rs73043098	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063471	chr19:38734744-39148392	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	73 gene(s)	inside rSNPs	diseases
2	nsv833822	chr19:38760748-38945105	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:38756600-38772600	Weak transcription	Primary T cells from cord blood	blood
2	chr19:38756600-38772600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr19:38756800-38772600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr19:38756800-38774800	Weak transcription	Primary B cells from peripheral blood	blood
5	chr19:38756800-38775000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr19:38756800-38778600	Weak transcription	Thymus	Thymus
7	chr19:38756800-38779600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr19:38758000-38770800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr19:38758000-38770800	Weak transcription	Primary B cells from cord blood	blood
10	chr19:38758000-38774200	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr19:38758200-38770800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr19:38758400-38774400	Weak transcription	Primary hematopoietic stem cells	blood
13	chr19:38758800-38770600	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr19:38759000-38768000	Weak transcription	Esophagus	oesophagus
15	chr19:38759000-38770800	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr19:38759400-38770800	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr19:38759600-38783200	Weak transcription	Fetal Brain Male	brain
18	chr19:38759800-38768200	Weak transcription	Fetal Kidney	kidney
19	chr19:38760800-38766000	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr19:38761200-38769000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr19:38761400-38770600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr19:38761600-38766800	Weak transcription	NHLF	lung
23	chr19:38761600-38767400	Strong transcription	NHEK	skin
24	chr19:38761600-38767800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr19:38761600-38767800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr19:38761600-38767800	Weak transcription	HSMM	muscle
27	chr19:38761600-38767800	Weak transcription	HSMMtube	muscle
28	chr19:38761600-38768200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr19:38761600-38768800	Weak transcription	Fetal Thymus	thymus
30	chr19:38761600-38769000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr19:38761600-38770800	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr19:38761600-38770800	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr19:38761600-38773000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr19:38761800-38767400	Weak transcription	NHDF-Ad	bronchial
35	chr19:38761800-38767600	Weak transcription	Osteobl	bone
36	chr19:38761800-38767800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr19:38761800-38768400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr19:38761800-38770800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr19:38764200-38768600	Weak transcription	Fetal Stomach	stomach
40	chr19:38764400-38766200	Enhancers	Lung	lung
41	chr19:38764400-38767800	Weak transcription	Spleen	Spleen
42	chr19:38764400-38771200	Weak transcription	Liver	Liver
43	chr19:38764600-38768200	Weak transcription	HepG2	liver
44	chr19:38764800-38766200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr19:38764800-38768800	Enhancers	Fetal Heart	heart
46	chr19:38765000-38766400	Enhancers	Brain Cingulate Gyrus	brain
47	chr19:38765000-38767000	Enhancers	Aorta	Aorta
48	chr19:38765200-38766000	Enhancers	Brain Anterior Caudate	brain
49	chr19:38765200-38766000	Enhancers	Brain Substantia Nigra	brain
50	chr19:38765200-38766200	Enhancers	Brain Hippocampus Middle	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links